A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602711



Internal ID20975782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50753032..50758267hg38UCSC Ensembl
chr7:50820729..50825964hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg385236
hg195236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157585
Samples
Known GenesGRB10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602711
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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